# FDA Inspection 1029762 - Delta Med SpA - October 26, 2017

Source: https://www.keypedia.com/records/fda_inspections/delta-med-spa/701a44fd-d8dc-4509-bb10-baa87bec3c0e
Source feed: FDA_Inspections

> FDA Inspection 1029762 for Delta Med SpA on October 26, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1029762
- Company Name: Delta Med SpA
- Inspection Date: 2017-10-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1029762 - 2017-10-26](https://www.keypedia.com/records/fda_inspections/delta-med-spa/ecffd11a-5eb7-4261-8c2e-28c01ea534c5)
- [FDA Inspection 780033 - 2012-05-03](https://www.keypedia.com/records/fda_inspections/delta-med-spa/d701ca5d-a8a7-44f5-a2f9-206a85047023)
- [FDA Inspection 780033 - 2012-05-03](https://www.keypedia.com/records/fda_inspections/delta-med-spa/7f9aa73a-e344-4955-912d-ace0f834ed31)

Company: https://www.keypedia.com/companies/delta-med-spa/0f883efb-8062-4c4d-b9bb-d4b4f468fe6d

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7